Search Results - "Altunbuker, Hira"

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  1. 1

    Clinical evaluation of muscle functions in neurofibromatosis type 1 by Gurler, Gokce, Altunbuker, Hira, Cankaya, Ozge, Esen‐Aydinli, Fatma, Incebay, Onal, Sel, Sinem A., Lay, Incilay, Kerem‐Gunel, Mintaze, Anlar, Banu

    Published in Journal of paediatrics and child health (01-11-2022)
    “…Aim Muscle weakness, fatigue and speech problems can occur in neurofibromatosis type 1 (NF1). The pathogenesis of these symptoms is unclear, likely…”
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    Journal Article
  2. 2

    Incidentally exploring natural course of a rare entity: representative case for rosette-forming glioneuronal tumors by Altunbüker, Hira, Hinz, Felix, Sahm, Felix, Brehmer, Stefanie, Wenz, Holger

    Published in Neurological sciences (01-10-2023)
    “…Rosette-forming glioneuronal tumors (RGNT) are extremely rare mostly benign tumors of the central nervous system, which are often studied for its histological…”
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    Journal Article
  3. 3

    Griscelli syndrome: Erdheim-Chester disease-like local presentation progressing to accelerated phase by Solakoğlu, Taha, Sönmez, Gamze, Kutay Tenekeci, Ateş, Altunbüker, Hira, Akar, Halil Tuna, Tezcan, Feyzi İlhan, Çağdaş Ayvaz, Deniz

    Published in Turkish journal of pediatrics (26-11-2024)
    “…Background. Griscelli syndrome (GS) is a rare genetic disorder characterized by oculocutaneous albinism and variable immune dysfunction. Among three distinct…”
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    Journal Article